<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Stefan Wiemann</submitter><organism>Homo sapiens</organism><software>Rnbeads (v.2.21.3)</software><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-15519</full_dataset_link><description>MCF7 (parental) cells were cultivated in estrogen deprived media for 12 months (long-term estrogen deprivation - LTED), until they had regained proliferative capacity (proxy for resistance to aromatase inhibition). Methylomes of parental and LTED MCF7 cells were analyzed to identify differentially methylated regions.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Scaning - Quality control, filtering and normalization were performed using Rnbeads (v.2.21.3)</sample_protocol><sample_protocol>Sample Treatment - MCF7 long term estrogen deprived (LTED) cells were cultivated in media lacking estrogen and phenol red.</sample_protocol><sample_protocol>Hybridization - Methylation profiling was performed by the DKFZ Microarray Core Facility using the Illumina MethylationEPIC BeadChip platform (Illumina, San Diego, CA, USA).</sample_protocol><sample_protocol>Sample Collection - Parental MCF7 cells were cultivated in Dulbecco’s Modified Eagle Medium (DMEM) supplemented with 10% FCS, 50 units/mL penicillin, 50 µg/mL streptomycin sulfate (Invitrogen AG, Carlsbad, CA, USA) and incubated at 37°C with 5% CO2 in a humidified incubator. Media was supplemented with 10−8 M 17-ß-estradiol (E2, Sigma-Aldrich, Saint-Louis, MI, USA) for cultivation of MCF7 parental cell parental line. Long-term estrogen-deprived (LTED) cells were cultured for one year in estrogen-free DMEM (w/o phenolred) supplemented with 10% charcoal-stripped FCS until the cells had regained proliferative capacities similar to parental MCF7 cells.</sample_protocol><sample_protocol>Nucleic Acid Extraction - Total DNA was extracted from MCF7 parental and LTED cells using the DNeasy Blood and Tissue Kit (Qiagen, Hilden, Germany), following the manufacturer’s protocol.</sample_protocol><sample_protocol>Labeling - Methylation profiling was performed by the DKFZ Microarray Core Facility using the Illumina MethylationEPIC BeadChip platform (Illumina, San Diego, CA, USA).</sample_protocol><figure_sub>MIAME Score</figure_sub><figure_sub>Raw Data</figure_sub><figure_sub>Organization</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><figure_sub>Array Designs</figure_sub><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><instrument_platform>Illumina MethylationEPIC BeadChip platform (Illumina, San Diego, CA, USA)</instrument_platform><study_type>methylation profiling by array</study_type><species>Homo sapiens</species><pubmed_authors>Stefan Wiemann</pubmed_authors></additional><is_claimable>false</is_claimable><name>Methylome profiling of MCF7 parental and long-term estrogen deprived cell lines</name><description>MCF7 (parental) cells were cultivated in estrogen deprived media for 12 months (long-term estrogen deprivation - LTED), until they had regained proliferative capacity (proxy for resistance to aromatase inhibition). Methylomes of parental and LTED MCF7 cells were analyzed to identify differentially methylated regions.</description><dates><release>2025-10-27T00:00:00Z</release><modification>2025-10-27T02:02:11.468Z</modification><creation>2025-08-29T11:20:33.82Z</creation></dates><accession>E-MTAB-15519</accession><cross_references><EFO>EFO_0002944</EFO><EFO>EFO_0003814</EFO><EFO>EFO_0003813</EFO><EFO>EFO_0002759</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003815</EFO><EFO>EFO_0003969</EFO></cross_references></HashMap>